HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitric Acid → 6-Chloro-3-nitro-imidazo(1,2-b)pyridazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Imidazo(1,2-b)pyridazine, 6-chloro- | HCID 138828 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 6-Chloro-3-nitro-imidazo(1,2-b)pyridazine | HCID 10535981 | 91% |
Reaction Steps
6-Chloroimidazo[1,2-b]pyridazine (4.95 g, 31.6 mmol) [purchased from Combi-Blocks] was dissolved in 60 mL concentrated sulfuric acid, cooled in an ice bath, and nitric acid (9.9 mL, 158 mmol) was added dropwise while stirring. The reaction was stirred at 0° C. for 30 minutes, then at ambient temperature for 4.5 hours to reach completion. The reaction was poured onto ice, and the resulting aqueous mixture was neutralized with 50% NaOH aqueous solution and then extracted with EtOAc (3×400 mL). The organic layers were combined and washed with water (2×400 mL) and brine (400 mL), dried (Na2SO4), filtered and concentrated to yield the product as a yellowish powder (5.7 g, 91% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09227975B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-c951cea0143b4d58a4d3b65caf39e348 |
| Source note | uspto-grants-2016_01 |